AutoICD API

Q11.2

Billable

Microphthalmos

Microphthalmos

Status

Billable / Specific

Parent Code

Q11

ICD-11 Mapping

1 equivalent

Coding Notes

Inclusion Terms

Alternative clinical terms for this condition

  • Cryptophthalmos NOS
  • Dysplasia of eye
  • Hypoplasia of eye
  • Rudimentary eye

Excludes 1

Codes that cannot be used together with this code (mutual exclusion)

Excludes 2

Conditions not included here, but the patient may have both

Related Codes(3)
Q11.0

Cystic eyeball

BillableQ11.1

Other anophthalmos

BillableQ11.3

Macrophthalmos

Billable
ICD-11 Equivalents(1)

ICD-11 Equivalents

View full mapping

Corresponding ICD-11 codes from the WHO crosswalk mapping

LA10.0MicrophthalmosequivalentPrimary
Also Known As / Clinical Terms(276)

SNOMED CT

UMLS

Clinical Terms

  • Coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness syndrome
  • Nanophthalmos, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
  • MIDAS syndrome
  • Microphthalmos due to Fryns syndrome
  • Globe of eye small
  • Bilateral microphthalmos
  • Viljoen Smart syndrome
  • Complete deafness
  • Syndromic nanophthalmos due to Kenny-Caffey syndrome
  • Ankyloblepharon
  • Hyposmia, nasal and ocular hypoplasia, hypogonadotropic hypogonadism syndrome
  • Syndromic microphthalmia type 6
  • Microphthalmia with ankyloblepharon and intellectual disability syndrome
  • Exognathia
  • Syndromic microphthalmia type 8
  • Blepharosynechia
  • Cryptophthalmos (disorder)
  • Cryptophthalmia
  • Bilateral cryptophthalmia
  • MIDAS syndrome (microphthalmia, dermal aplasia, sclerocornea) syndrome
  • Bosma arhinia microphthalmia syndrome
  • Truncal obesity
  • Bilateral colobomatous microphthalmia
  • Colobomatous microphthalmia, obesity, hypogenitalism, intellectual disability syndrome
  • Median cleft face syndrome
  • cryptophthalmos
  • Microphthalmos due to branchio-oculo-facial syndrome
  • Bosma Henkin Christiansen syndrome
  • Congenital absence of lens
  • Congenital cryptophthalmos of bilateral eyelids
  • Microphthalmia, coloboma, rhizomelic skeletal dysplasia
  • COMMAD (coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, deafness) syndrome
  • Big jaw
  • Mackay Shek Carr syndrome
  • Microphthalmia with colobomatous cyst
  • Congenital hypoplasia of nose
  • Optic nerve head drusen
  • Akinesia
  • Congenital small nose
  • Retinal degeneration, nanophthalmos, glaucoma syndrome
  • Central obesity
  • Microphthalmos (disorder)
  • Isolated cryptophthalmos
  • Microphthalmia with linear skin defect syndrome
  • Ankyloblepharon totale
  • Obesity of face and trunk, sparing limbs
  • Microphthalmos of bilateral eyes
  • X-linked colobomatous microphthalmia, microcephaly, intellectual disability, short stature syndrome
  • Dysplasia of eye (disorder)
  • Congenital microphthalmos
  • Progenia
  • Microphthalmia with brain atrophy syndrome
  • Congenital prognathism
  • Microphthalmos of right eye
  • Microphthalmia, retinitis pigmentosa, foveoschisis, optic disc drusen syndrome
  • Bilateral cryptophthalmos
  • Microphthalmia
  • Syndromic microphthalmia type 5
  • Thomas Jewett Raines syndrome
  • Microphthalmic socket
  • Bakrania Ragge syndrome
  • ALX1-related frontonasal dysplasia
  • Nanophthalmos
  • Congenital blindness
  • Partial cryptophthalmos of both eyelids
  • Microphthalmia of left eye
  • Microtia
  • Partial cryptophthalmos of bilateral eyelids
  • Prognathism
  • Complete cryptophthalmos
  • Microphthalmos of both eyes
  • Simple microphthalmos (disorder)
  • Syndromic microphthalmia type 7
  • Lenz microphthalmia syndrome
  • Hyaline bodies of optic disc
  • Cryptophthalmos NOS
  • Frontonasal dysplasia type 3
  • Teebi Al Saleh Hassoon syndrome
  • Congenital hypoplastic nose
  • Microphthalmos of left eye
  • Prognathia
  • ALX1 (aristaless-like homeobox 1) related frontonasal dysplasia
  • Microphthalmia of right eye
  • Dysplasia of eye
  • Congenital aphakia
  • Bilateral partial cryptophthalmos
  • MMEP syndrome
  • Colobomatous microphthalmia
  • Isolated cryptophthalmia
  • Centripetal obesity
  • Colobomatous microphthalmia, rhizomelic dysplasia syndrome
  • Hypoplasia of eye
  • Microphthalmos due to Delleman syndrome
  • Congenital cryptophthalmos of both eyelids
  • MOBA syndrome
  • Microcephaly, microphthalmia, ectrodactyly of lower limbs and prognathism syndrome
  • Microphthalmos, unspecified
  • Congenital deafness
  • Microphthalmia, microtia, fetal akinesia syndrome
  • Nanophthalmia
  • Rudimentary eye
  • Microphthalmia with brain and digit anomaly
  • Frontonasal dysplasia sequence
  • Congenital ankyloblepharon
  • X-linked colobomatous microphthalmia, microcephaly, short stature, psychomotor retardation syndrome
  • Fused eyelids
  • Macrosomia, microphthalmia, cleft palate syndrome
  • COMMAD syndrome
  • Hypoplasia of eye (disorder)
  • Drusen of optic disc
  • Agenesis of lens
  • Syndromic microphthalmia type 10
  • Frontonasal dysplasia, severe microphthalmia, severe facial clefting syndrome
  • Simple microphthalmos
  • Android fat distribution
  • Fat body with thin limbs
  • Syndromic microphthalmia type 4
  • Syndromic microphthalmia due to OTX2 mutation
  • Syndromic microphthalmia due to orthodenticle homeobox 2 mutation
  • Microphthalmos co-occurrent with congenital ocular coloboma
  • Complete cryptophthalmia
  • Optic disc drusen
  • Microphthalmos with congenital ocular coloboma of both eyes
  • Congenital aphakia, iris hypoplasia, microphthalmia, microcornea syndrome
  • Congenital small ears
  • Microphthalmos co-occurrent with congenital ocular coloboma of bilateral eyes
  • Bilateral microphthalmos with congenital coloboma
  • Small eyeball
  • Microphthalmia, microtia, foetal akinesia syndrome
Frequently Asked Questions
What is the ICD-10 code for microphthalmos?

The ICD-10-CM code for microphthalmos is Q11.2. The full clinical description is "Microphthalmos". Q11.2 is a billable/specific code that can be used on insurance claims and medical billing.

What does ICD-10 code Q11.2 mean?

ICD-10-CM code Q11.2 represents “Microphthalmos”. It is classified under Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities and is a billable/specific code that can be used on a claim.

Is Q11.2 a billable code?

Yes, Q11.2 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.

What chapter is Q11.2 in?

Q11.2 is in Chapter 17: Congenital Malformations, Deformations and Chromosomal Abnormalities (codes Q00-Q99).

What codes cannot be used with Q11.2?

Q11.2 has Excludes1 notes indicating codes that cannot be used together with it, including: cryptophthalmos syndrome (Q87.0).

What SNOMED CT codes does Q11.2 map to?

Q11.2 maps to 51 SNOMED CT concepts: 773628009, 35387008, 33994004, 248311001, 193953008, and 46 more. SNOMED CT is a clinical terminology used in electronic health records.

What are the UMLS CUIs for Q11.2?

Q11.2 is linked to 4 UMLS Concept Unique Identifiers: C0026010, C0311249, C0266524, C0266527. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.

How does Q11.2 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like microphthalmos affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of Q11.2?

Q11.2 maps to the ICD-11 code: LA10.0 (Microphthalmos).

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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.